Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Mercedes Maceiras"'
Autor:
Celeste Mattone, Gabriela Guercio, Maria Sol Touzon, Jose Garcia-Feyling, Mariana Costanzo, Mercedes Maceiras, Roxana Marino, N. Saraco, Hellem Carolina Patiño, Gisela Viterbo, Alicia Belgorosky, Natalia Perez Garrido, Juan Manuel Lazzati
Publikováno v:
Hormone Research in Paediatrics. 90:275-282
Background: Aromatase deficiency is a rare autosomal recessive disorder. 46,XY-affected patients often remain undiagnosed until late puberty. Only 2 pediatric cases have been reported. Data on pubertal development in affected males are scarce. Aim: T
Autor:
Juan Manuel Lazzati, Viviana Herzovich, Mercedes Maceiras, Natalia Gazek, Noelia Dujovne, Alicia Belgorosky
Publikováno v:
Archivos argentinos de pediatria. 117(6)
Hypothyroidism caused by Hashimoto's thyroiditis is the most common reason for thyroid dysfunction in children. Our objective was to analyze its impact on final stature in relation to height and pubertal stage at the time of diagnosis in children you
Autor:
Melina Pelanda, Viviana Herzovich, Veronica Zaidman, Eduardo Chaler, Juan Manuel Lazzati, Alicia Belgorosky, Alejandra Ribas, Mercedes Maceiras
Publikováno v:
Clinical chemistry and laboratory medicineReferences. 56(6)
Healthcare budgets worldwide are facing increasing pressureto reduce costs and improve efficiency, while maintainingquality. Laboratory testing has not escaped thispressure.The clinical laboratory control of demand is oftenconfused with demand manage
Autor:
Marco A. Rivarola, Elisa Vaiani, Eduardo Chaler, Alicia Belgorosky, Mariana Costanzo, Esperanza Berensztein, Mercedes Maceiras, Gabriela Guercio, Pablo Ramírez, María Sonia Baquedano, Marcela Bailez, Roxana Marino
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 98:E153-E161
Steroid acute regulatory (StAR) protein is a mitochondria-targeted protein that is part of the transduceosome complex crucial for transport of cholesterol to mitochondria. Recessive mutations cause classic and nonclassic congenital lipoid adrenal hyp
Autor:
Matías, Juanes, Isabel, Di Palma, Marta, Ciaccio, Roxana, Marino, Pablo C, Ramírez, Natalia, Pérez Garrid, Mercedes, Maceiras, Juan M, Lazzati, Marco A, Rivarola, Alicia, Belgorosky
Publikováno v:
Medicina. 76(4)
Several heterozygous GLI2 gene mutations have been reported in patients with isolated GH deficiency (IGHD) or multiple pituitary hormone deficiency (MPHD) with or without other malformations. The primary aim of this study was to analyze the presence
The responsibility of clinical laboratories includes adequate assay methods, measurement procedures, and the definition of the appropriate quality specifications for each mensurand as well as the identification of criteria required for obtaining the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23c6dc3a5101af352d9c973cf306809a
https://www.degruyter.com/view/j/cclm.2016.54.issue-11/cclm-2015-0954/cclm-2015-0954.xml
https://www.degruyter.com/view/j/cclm.2016.54.issue-11/cclm-2015-0954/cclm-2015-0954.xml
Autor:
Mariana Prieto, Andrea G. Krochik, Eduardo Chaler, Mercedes Maceiras, Anabel Villalba, Silvina Valdez, Gloria Cerrone, Mariana Telechea, Carmen Mazza
Publikováno v:
Medicina (Buenos Aires), Vol 72, Iss 4, Pp 291-297 (2012)
Los cambios en la forma de presentación de la diabetes mellitus tipo 1(DM T1) en la infancia y adolescencia asociados a la obesidad, determinaron una superposición entre los dos tipos de diabetes, con mayor heterogeneidad en su presentación clíni
Autor:
Mariana Prieto, Andrea G. Krochik, Eduardo Chaler, Mercedes Maceiras, Anabel Villalba, Silvina Valdez, Gloria Cerrone, Mariana Telechea, Carmen Mazza
Publikováno v:
Medicina (Buenos Aires), Vol 72, Iss 4, Pp 291-297 (2012)
Los cambios en la forma de presentación de la diabetes mellitus tipo 1(DM T1) en la infancia y adolescencia asociados a la obesidad, determinaron una superposición entre los dos tipos de diabetes, con mayor heterogeneidad en su presentación clíni
Autor:
María Sonia Baquedano, Mariana Costanzo, Roxana Marino, Marco A. Rivarola, Mercedes Maceiras, Gabriela Guercio, Eduardo Chaler, Esperanza Berensztein, Juan Manuel Lazzatti, Alicia Belgorosky, Pablo Ramirez, Jessica Galeano, Nora Saraco, Diana Monica Warman, Valeria De Dona, Marta Ciaccio
Publikováno v:
Hormone Research in Paediatrics. 78:119-126
In humans, steroidogenic factor 1 (NR5A1/SF-1) mutations have been reported to cause gonadal dysgenesis, with or without adrenal failure, in both 46,XY and 46,XX individuals. We have previously reported extreme within-family variability in affected 4
Autor:
Marco A. Rivarola, Esperanza Berensztein, Nora Saraco, Eduardo Chaler, Gabriela Guercio, Diana Monica Warman, Marta Ciaccio, Pablo Ramirez, Juan Manuel Lazzatti, María Sonia Baquedano, Alicia Belgorosky, Mariana Costanzo, Jesica Galeano, Roxana Marino, Marcela Bailez, Mercedes Maceiras
Publikováno v:
Hormone Research in Paediatrics. 75:70-77
Background: Three novel heterozygous SF-1 gene mutations affecting multiple members of two unrelated families with a history of 46,XY disorders of sex development (DSD) and 46,XX ovarian insufficiency are described. Methods: Clinical and mutational a